# autosomal recessive nonsyndromic deafness 22

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the OTOA gene on chromosome 16p12

**Wikidata**: [Q28024605](https://www.wikidata.org/wiki/Q28024605)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-22


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)